JPS5871926A - 弾性ポリエ−テルエステルイミド及びその製造方法 - Google Patents

弾性ポリエ−テルエステルイミド及びその製造方法

Info

Publication number: JPS5871926A
Authority: JP; Japan
Prior art keywords: glycol; molecular weight; esterimide; poly; polyether
Prior art date: 1981-10-02
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Pending

Application number

JP57168689A

Other languages

English (en)

Japanese (ja)

Inventor

ジエ−ムズ・リチヤ−ド・ウルフ・ジユニア

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

EIDP Inc

Original Assignee

EI Du Pont de Nemours and Co

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1981-10-02

Filing date

1982-09-29

Publication date

1983-04-28

1982-09-29 Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co

1983-04-28 Publication of JPS5871926A publication Critical patent/JPS5871926A/ja

Status Pending legal-status Critical Current

Links

-1 ester imide Chemical class 0.000 title claims description 40
239000004721 Polyphenylene oxide Substances 0.000 title claims description 18
229920000570 polyether Polymers 0.000 title claims description 18
238000004519 manufacturing process Methods 0.000 title claims description 5
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 70
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 26
SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 claims description 20
150000002009 diols Chemical class 0.000 claims description 16
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 11
150000004985 diamines Chemical class 0.000 claims description 11
DZIHTWJGPDVSGE-UHFFFAOYSA-N 4-[(4-aminocyclohexyl)methyl]cyclohexan-1-amine Chemical compound C1CC(N)CCC1CC1CCC(N)CC1 DZIHTWJGPDVSGE-UHFFFAOYSA-N 0.000 claims description 9
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 8
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims description 8
229920000233 poly(alkylene oxides) Polymers 0.000 claims description 7
239000000203 mixture Substances 0.000 claims description 6
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 5
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
125000003277 amino group Chemical group 0.000 claims description 4
RTWNYYOXLSILQN-UHFFFAOYSA-N methanediamine Chemical compound NCN RTWNYYOXLSILQN-UHFFFAOYSA-N 0.000 claims description 4
229920001169 thermoplastic Polymers 0.000 claims description 2
239000004416 thermosoftening plastic Substances 0.000 claims description 2
229920001451 polypropylene glycol Polymers 0.000 claims 1
229920000642 polymer Polymers 0.000 description 57
238000006116 polymerization reaction Methods 0.000 description 19
239000011347 resin Substances 0.000 description 12
229920005989 resin Polymers 0.000 description 12
238000000034 method Methods 0.000 description 11
150000002148 esters Chemical class 0.000 description 10
239000011521 glass Substances 0.000 description 9
239000000178 monomer Substances 0.000 description 9
239000003054 catalyst Substances 0.000 description 8
230000008569 process Effects 0.000 description 8
238000009833 condensation Methods 0.000 description 7
230000005494 condensation Effects 0.000 description 7
235000019589 hardness Nutrition 0.000 description 7
239000000047 product Substances 0.000 description 7
238000012360 testing method Methods 0.000 description 7
238000005299 abrasion Methods 0.000 description 6
125000001931 aliphatic group Chemical group 0.000 description 6
239000003963 antioxidant agent Substances 0.000 description 6
238000009835 boiling Methods 0.000 description 6
229960004063 propylene glycol Drugs 0.000 description 6
DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 5
239000002253 acid Substances 0.000 description 5
230000006835 compression Effects 0.000 description 5
238000007906 compression Methods 0.000 description 5
150000002334 glycols Chemical class 0.000 description 5
238000000227 grinding Methods 0.000 description 5
235000013772 propylene glycol Nutrition 0.000 description 5
239000011541 reaction mixture Substances 0.000 description 5
239000003381 stabilizer Substances 0.000 description 5
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
150000001412 amines Chemical class 0.000 description 4
230000003078 antioxidant effect Effects 0.000 description 4
238000006243 chemical reaction Methods 0.000 description 4
238000001816 cooling Methods 0.000 description 4
229910000071 diazene Inorganic materials 0.000 description 4
238000001914 filtration Methods 0.000 description 4
238000005259 measurement Methods 0.000 description 4
239000000155 melt Substances 0.000 description 4
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
239000002904 solvent Substances 0.000 description 4
229920002725 thermoplastic elastomer Polymers 0.000 description 4
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
229920001577 copolymer Polymers 0.000 description 3
150000005690 diesters Chemical class 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
150000002989 phenols Chemical class 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
238000012545 processing Methods 0.000 description 3
239000000376 reactant Substances 0.000 description 3
238000010992 reflux Methods 0.000 description 3
239000000243 solution Substances 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 2
230000009471 action Effects 0.000 description 2
YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 2
238000003490 calendering Methods 0.000 description 2
238000000576 coating method Methods 0.000 description 2
238000005520 cutting process Methods 0.000 description 2
230000007423 decrease Effects 0.000 description 2
RAABOESOVLLHRU-UHFFFAOYSA-N diazene Chemical compound N=N RAABOESOVLLHRU-UHFFFAOYSA-N 0.000 description 2
238000001035 drying Methods 0.000 description 2
229920001971 elastomer Polymers 0.000 description 2
239000000806 elastomer Substances 0.000 description 2
230000032050 esterification Effects 0.000 description 2
238000005886 esterification reaction Methods 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
230000001788 irregular Effects 0.000 description 2
239000000463 material Substances 0.000 description 2
238000000465 moulding Methods 0.000 description 2
230000000704 physical effect Effects 0.000 description 2
229910001220 stainless steel Inorganic materials 0.000 description 2
239000010935 stainless steel Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
238000010189 synthetic method Methods 0.000 description 2
238000010998 test method Methods 0.000 description 2
229910052719 titanium Inorganic materials 0.000 description 2
239000010936 titanium Substances 0.000 description 2
ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
MJHNUUNSCNRGJE-UHFFFAOYSA-N trimethyl benzene-1,2,4-tricarboxylate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C(C(=O)OC)=C1 MJHNUUNSCNRGJE-UHFFFAOYSA-N 0.000 description 2
SPDQEKZIKVLFRJ-UHFFFAOYSA-N 1,13-dichlorotridecane-3,11-diamine Chemical compound NC(CCCCCCCC(CCCl)N)CCCl SPDQEKZIKVLFRJ-UHFFFAOYSA-N 0.000 description 1
VETPHHXZEJAYOB-UHFFFAOYSA-N 1-n,4-n-dinaphthalen-2-ylbenzene-1,4-diamine Chemical compound C1=CC=CC2=CC(NC=3C=CC(NC=4C=C5C=CC=CC5=CC=4)=CC=3)=CC=C21 VETPHHXZEJAYOB-UHFFFAOYSA-N 0.000 description 1
BWRZUFCHMYMKPK-UHFFFAOYSA-N 1-o-butyl 3-o-[(3,5-ditert-butyl-4-hydroxyphenyl)methyl] propanedioate Chemical compound CCCCOC(=O)CC(=O)OCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 BWRZUFCHMYMKPK-UHFFFAOYSA-N 0.000 description 1
DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 description 1
QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
ODJQKYXPKWQWNK-UHFFFAOYSA-N 3,3'-Thiobispropanoic acid Chemical compound OC(=O)CCSCCC(O)=O ODJQKYXPKWQWNK-UHFFFAOYSA-N 0.000 description 1
FJDLQLIRZFKEKJ-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanamide Chemical compound CC(C)(C)C1=CC(CCC(N)=O)=CC(C(C)(C)C)=C1O FJDLQLIRZFKEKJ-UHFFFAOYSA-N 0.000 description 1
VWQJDBDBKBVVBX-UHFFFAOYSA-N 3-tert-butyl-4-[1-(2-tert-butyl-4-hydroxy-6-methylphenyl)butyl]-5-methylphenol Chemical compound CC=1C=C(O)C=C(C(C)(C)C)C=1C(CCC)C1=C(C)C=C(O)C=C1C(C)(C)C VWQJDBDBKBVVBX-UHFFFAOYSA-N 0.000 description 1
UJAWGGOCYUPCPS-UHFFFAOYSA-N 4-(2-phenylpropan-2-yl)-n-[4-(2-phenylpropan-2-yl)phenyl]aniline Chemical compound C=1C=C(NC=2C=CC(=CC=2)C(C)(C)C=2C=CC=CC=2)C=CC=1C(C)(C)C1=CC=CC=C1 UJAWGGOCYUPCPS-UHFFFAOYSA-N 0.000 description 1
VSAWBBYYMBQKIK-UHFFFAOYSA-N 4-[[3,5-bis[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]-2,4,6-trimethylphenyl]methyl]-2,6-ditert-butylphenol Chemical compound CC1=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C1CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 VSAWBBYYMBQKIK-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
KEQFTVQCIQJIQW-UHFFFAOYSA-N N-Phenyl-2-naphthylamine Chemical compound C=1C=C2C=CC=CC2=CC=1NC1=CC=CC=C1 KEQFTVQCIQJIQW-UHFFFAOYSA-N 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
239000003490 Thiodipropionic acid Substances 0.000 description 1
ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 1
QLBRROYTTDFLDX-UHFFFAOYSA-N [3-(aminomethyl)cyclohexyl]methanamine Chemical compound NCC1CCCC(CN)C1 QLBRROYTTDFLDX-UHFFFAOYSA-N 0.000 description 1
FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
239000000654 additive Substances 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
230000008901 benefit Effects 0.000 description 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
239000012965 benzophenone Substances 0.000 description 1
150000008366 benzophenones Chemical class 0.000 description 1
150000001565 benzotriazoles Chemical class 0.000 description 1
VSGNNIFQASZAOI-UHFFFAOYSA-L calcium acetate Chemical compound [Ca+2].CC([O-])=O.CC([O-])=O VSGNNIFQASZAOI-UHFFFAOYSA-L 0.000 description 1
239000001639 calcium acetate Substances 0.000 description 1
235000011092 calcium acetate Nutrition 0.000 description 1
229960005147 calcium acetate Drugs 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000004927 clay Substances 0.000 description 1
229910052570 clay Inorganic materials 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000011437 continuous method Methods 0.000 description 1
229930003836 cresol Natural products 0.000 description 1
VKIRRGRTJUUZHS-UHFFFAOYSA-N cyclohexane-1,4-diamine Chemical compound NC1CCC(N)CC1 VKIRRGRTJUUZHS-UHFFFAOYSA-N 0.000 description 1
VKONPUDBRVKQLM-UHFFFAOYSA-N cyclohexane-1,4-diol Chemical compound OC1CCC(O)CC1 VKONPUDBRVKQLM-UHFFFAOYSA-N 0.000 description 1
230000006378 damage Effects 0.000 description 1
FOTKYAAJKYLFFN-UHFFFAOYSA-N decane-1,10-diol Chemical class OCCCCCCCCCCO FOTKYAAJKYLFFN-UHFFFAOYSA-N 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
239000004744 fabric Substances 0.000 description 1
239000000835 fiber Substances 0.000 description 1
239000011152 fibreglass Substances 0.000 description 1
229920001973 fluoroelastomer Polymers 0.000 description 1
NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229920006158 high molecular weight polymer Polymers 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000011256 inorganic filler Substances 0.000 description 1
229910003475 inorganic filler Inorganic materials 0.000 description 1
239000004611 light stabiliser Substances 0.000 description 1
UEGPKNKPLBYCNK-UHFFFAOYSA-L magnesium acetate Chemical compound [Mg+2].CC([O-])=O.CC([O-])=O UEGPKNKPLBYCNK-UHFFFAOYSA-L 0.000 description 1
229940069446 magnesium acetate Drugs 0.000 description 1
235000011285 magnesium acetate Nutrition 0.000 description 1
239000011654 magnesium acetate Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
238000002156 mixing Methods 0.000 description 1
AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 1
239000002245 particle Substances 0.000 description 1
UWJJYHHHVWZFEP-UHFFFAOYSA-N pentane-1,1-diol Chemical compound CCCCC(O)O UWJJYHHHVWZFEP-UHFFFAOYSA-N 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920001983 poloxamer Polymers 0.000 description 1
229920003217 poly(methylsilsesquioxane) Polymers 0.000 description 1
238000012643 polycondensation polymerization Methods 0.000 description 1
238000006068 polycondensation reaction Methods 0.000 description 1
239000002685 polymerization catalyst Substances 0.000 description 1
238000003825 pressing Methods 0.000 description 1
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
238000001175 rotational moulding Methods 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
239000002893 slag Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000007790 solid phase Substances 0.000 description 1
238000009987 spinning Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000010959 steel Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
235000019303 thiodipropionic acid Nutrition 0.000 description 1
239000000052 vinegar Substances 0.000 description 1
235000021419 vinegar Nutrition 0.000 description 1
239000003039 volatile agent Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C08G73/16—Polyester-imides

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)

JP57168689A 1981-10-02 1982-09-29 弾性ポリエ−テルエステルイミド及びその製造方法 Pending JPS5871926A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US06/308,130 US4371692A (en)	1981-10-02	1981-10-02	Elastomeric polyetheresterimides
US308130		1981-10-02

Publications (1)

Publication Number	Publication Date
JPS5871926A true JPS5871926A (ja)	1983-04-28

Family

ID=23192678

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP57168689A Pending JPS5871926A (ja)	1981-10-02	1982-09-29	弾性ポリエ−テルエステルイミド及びその製造方法

Country Status (7)

Country	Link
US (1)	US4371692A (de)
EP (1)	EP0076482B1 (de)
JP (1)	JPS5871926A (de)
AU (1)	AU549410B2 (de)
CA (1)	CA1187648A (de)
DE (1)	DE3268976D1 (de)
ES (1)	ES8400458A1 (de)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS61108626A (ja) *	1984-10-26	1986-05-27	ゼネラル・エレクトリツク・カンパニイ	熱可塑性ポリエーテルイミドエステルエラストマー
JPS627734A (ja) *	1985-07-05	1987-01-14	Teijin Ltd	ガスバリアー性成形品の製造法
JPS62501365A (ja) *	1985-01-11	1987-06-04	ゼネラル・エレクトリック・カンパニイ	熱可塑性ポリエ−テルイミドエステルエラストマ−
JPS63152631A (ja) *	1986-11-10	1988-06-25	ゼネラル・エレクトリック・カンパニイ	ポリエーテルイミドエステル
JPS63199231A (ja) *	1986-12-02	1988-08-17	ゼネラル・エレクトリック・カンパニイ	改良された可撓性を示す熱可塑性ポリエーテルイミドエステルポリマーの製造方法
JPS63199232A (ja) *	1986-12-02	1988-08-17	ゼネラル・エレクトリック・カンパニイ	熱可塑性ポリエーテルイミドエステル
JP2006052275A (ja) *	2004-08-10	2006-02-23	Hitachi Chem Co Ltd	樹脂組成物、樹脂付き基材及び導体層張り積層板

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4594377A (en) *	1984-10-26	1986-06-10	General Electric Company	Modified thermoplastic copolyetherimide ester elastomers
US4544734A (en) *	1984-10-26	1985-10-01	General Electric Company	Modified thermoplastic copolyetherimide ester elastomers
EP0180149A3 (de) *	1984-10-26	1987-09-23	General Electric Company	Diimid-disäuren und Diimid-diester mit hohem Molekulargewicht hergestellt aus Tricarbonsäureanhydriden
US4552950A (en) *	1985-01-11	1985-11-12	General Electric Company	Polyetherimide esters
US4598117A (en) *	1985-01-11	1986-07-01	General Electric Company	Elastomeric compositions comprising a combination of (a) an aromatic thermoplastic polyester and (b) clay/syenite
US4659765A (en) *	1985-02-19	1987-04-21	General Electric Company	Elastomeric compositions
US4769475A (en) *	1985-03-19	1988-09-06	Nippon Telegraph And Telephone Corporation	Bis(hydroxyphthalimide) and process for preparing the same, and process for preparing polyesterimide by the use thereof
US4711933A (en) *	1986-11-10	1987-12-08	General Electric Company	Polyetherimide esters
US4731435A (en) *	1986-11-10	1988-03-15	E. I. Du Pont De Nemours And Company	Elastomers
US4810770A (en) *	1986-11-10	1989-03-07	E. I. Du Pont De Nemours And Company	Elastomers
US4732948A (en) *	1986-12-02	1988-03-22	General Electric Company	Solid phase polycondensation process for the production of high molecular weight polyetherimide ester polymers
US4732947A (en) *	1986-12-02	1988-03-22	General Electric Company	Block polyetherimide ester polymers
US4740565A (en) *	1986-12-02	1988-04-26	General Electric Company	Thermoplastic polyetherimide ester polymers exhibiting improved flexular properties
US4798858A (en) *	1987-03-04	1989-01-17	General Electric Company	Flame retardant polyetherimide ester elastomers
US4973658A (en) *	1987-12-31	1990-11-27	E. I. Du Pont De Nemours And Company	Thermoplastic copolyester elasatomer binder for oxidizer particles
US5003030A (en) *	1988-05-17	1991-03-26	Idemitsu Petrochemical Co., Ltd.	Thermoplastic wholly aromatic copolyimide ester and process for producing the same
CA2030645A1 (en) *	1990-01-02	1991-07-03	Harold F. Giles, Jr.	Polyamide fiber reinforced polyetherester composition
US5262493A (en) *	1990-06-29	1993-11-16	General Electric Company	Blow-moldable copolyethenimide kister compositions salts of aliphatic polycarboxylic acid
US5254640A (en) *	1990-06-29	1993-10-19	General Electric Company	Copolyetherimide ester compositions
US5110668A (en) *	1990-12-21	1992-05-05	General Electric Company	Flexible laminate having copolyetherester adhesive
US5883220A (en) *	1992-01-12	1999-03-16	Centre National De La Recherche Scientifique	Redox copolymers and their use in preparing mixed conduction materials
US5225485A (en) *	1992-03-03	1993-07-06	United States Surgical Corporation	Polyetherimide ester suture and its method of manufacture and method of use

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US3274159A (en) *	1963-01-07	1966-09-20	Union Carbide Corp	Polyester imides of trimellitic anhydride
DE1495174C2 (de) *	1964-04-25	1983-07-14	Dr. Beck & Co Ag, 2000 Hamburg	Verfahren zur Herstellung von hitzehärtbaren Polyesterharzen, die neben Estergruppen und fünfgliedrigen Imidringen innerhalb der Ketten noch Amidgruppen enthalten
US3852246A (en) *	1964-06-09	1974-12-03	Beck & Co Gmbh	Polyesterimide resins
BE793332A (fr) *	1972-01-26	1973-04-16	Du Pont	Copolyesters thermoplastiques a segments
JPS5234756B2 (de) *	1974-05-01	1977-09-05
US4205158A (en) *	1979-03-28	1980-05-27	E. I. Du Pont De Nemours And Company	Copolyetherester based on ethylene oxide-capped poly(propylene oxide) glycol and branching agent
DE2925582A1 (de) *	1979-06-25	1981-01-22	Basf Ag	Thermoplastische, segmentierte elastomere copolyaetherester und ihre verwendung als haftkleber

1981
- 1981-10-02 US US06/308,130 patent/US4371692A/en not_active Expired - Lifetime
1982
- 1982-09-22 ES ES515874A patent/ES8400458A1/es not_active Expired
- 1982-09-29 JP JP57168689A patent/JPS5871926A/ja active Pending
- 1982-09-30 AU AU88933/82A patent/AU549410B2/en not_active Ceased
- 1982-09-30 CA CA000412612A patent/CA1187648A/en not_active Expired
- 1982-10-01 DE DE8282109076T patent/DE3268976D1/de not_active Expired
- 1982-10-01 EP EP82109076A patent/EP0076482B1/de not_active Expired

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS61108626A (ja) *	1984-10-26	1986-05-27	ゼネラル・エレクトリツク・カンパニイ	熱可塑性ポリエーテルイミドエステルエラストマー
JPS62501365A (ja) *	1985-01-11	1987-06-04	ゼネラル・エレクトリック・カンパニイ	熱可塑性ポリエ−テルイミドエステルエラストマ−
JPS627734A (ja) *	1985-07-05	1987-01-14	Teijin Ltd	ガスバリアー性成形品の製造法
JPS63152631A (ja) *	1986-11-10	1988-06-25	ゼネラル・エレクトリック・カンパニイ	ポリエーテルイミドエステル
JPS63199231A (ja) *	1986-12-02	1988-08-17	ゼネラル・エレクトリック・カンパニイ	改良された可撓性を示す熱可塑性ポリエーテルイミドエステルポリマーの製造方法
JPS63199232A (ja) *	1986-12-02	1988-08-17	ゼネラル・エレクトリック・カンパニイ	熱可塑性ポリエーテルイミドエステル
JP2006052275A (ja) *	2004-08-10	2006-02-23	Hitachi Chem Co Ltd	樹脂組成物、樹脂付き基材及び導体層張り積層板

Also Published As

Publication number	Publication date
CA1187648A (en)	1985-05-21
AU8893382A (en)	1983-04-14
DE3268976D1 (en)	1986-03-20
ES515874A0 (es)	1983-11-01
ES8400458A1 (es)	1983-11-01
AU549410B2 (en)	1986-01-23
US4371692A (en)	1983-02-01
EP0076482B1 (de)	1986-02-05
EP0076482A1 (de)	1983-04-13

Publication	Publication Date	Title
JPS5871926A (ja)	1983-04-28	弾性ポリエ−テルエステルイミド及びその製造方法
EP0076483B1 (de)	1986-02-05	Thermoplastische elastomere Polyätheresterimide
CN110268004B (zh)	2022-07-01	聚酰胺-酰亚胺膜
KR830002015B1 (ko)	1983-10-06	산화에틸렌 결합 폴리(산화프로필렌)글리콜과 측쇄형성제의 중축합에 의한 코폴리에테르 에스테르
JPS5840977B2 (ja)	1983-09-09	熱可塑性ポリエステル共重合体エラストマ−の製造法
CN110325568B (zh)	2021-12-10	聚酰胺-酰亚胺膜的制备方法
JPH02248425A (ja)	1990-10-04	ポリ（１，３―プロピレンテレフタレート）の硬いセグメントをもつたポリエステルエーテル共重合体エラストマー
US4820796A (en)	1989-04-11	Transparent polyamide elastomer from carboxy polycaprolactam and poly(tetramethylene oxy)glycol
Han et al.	2002	Preparation and characterization of high molecular weight poly (butylene succinate)
NZ233733A (en)	1991-07-26	Elongated objects prepared from oriented olefine-carbon monoxide polymer having modulus of elasticity of at least 16 gpa
EP0203634B1 (de)	1989-08-30	Copolyätherester aus ethylenoxidblockiertem Polypropylenoxid
JPH0340057B2 (de)	1991-06-17
JP5223347B2 (ja)	2013-06-26	樹脂組成物及びその製造方法、並びに共重合体
JP3112943B2 (ja)	2000-11-27	ポリ−（１，３−プロピレン−４，４−ジフェニルジカルボキシレート）の硬質分画を有する共縮合ポリエーテルエステル弾性体
KR101161890B1 (ko)	2012-07-03	블록 코폴리에터에스터 엘라스토머 및 그의 제조방법
EP0268090A2 (de)	1988-05-25	Polyetherimidester
JP3100185B2 (ja)	2000-10-16	脂環式硬質セグメントを有するコポリエーテルエステルエラストマー
JPH07102062A (ja)	1995-04-18	ポリエーテルブロックとポリアミドブロックとからなるポリマー
JPS6218568B2 (de)	1987-04-23
EP1873184B1 (de)	2011-12-07	Polyetheresterblockcopolymer
Wang et al.	1996	Synthesis and characterization of new block copolyurethanes based on 1, 2-ethylene bis (4-phenylisocyanate)
WO2008064857A1 (en)	2008-06-05	Block-copolymer elastomer
TWI849651B (zh)	2024-07-21	共聚醯胺彈性體及其製備方法
Huang et al.	1998	Poly (amide‐ester) s from p‐aminobenzoic acid
JPS63301223A (ja)	1988-12-08	新規ポリエ−テル・エステル・アミド・ブロック・コポリマ−

JPS5871926A - 弾性ポリエ−テルエステルイミド及びその製造方法 - Google Patents

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